US5688885A - Tetrafluoroethylene terpolymer - Google Patents
Tetrafluoroethylene terpolymer Download PDFInfo
- Publication number
- US5688885A US5688885A US08/678,919 US67891996A US5688885A US 5688885 A US5688885 A US 5688885A US 67891996 A US67891996 A US 67891996A US 5688885 A US5688885 A US 5688885A
- Authority
- US
- United States
- Prior art keywords
- hfp
- tfe
- pmve
- hfpi
- copolymer
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired - Lifetime
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Classifications
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F214/00—Copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by a halogen
- C08F214/18—Monomers containing fluorine
- C08F214/26—Tetrafluoroethene
- C08F214/262—Tetrafluoroethene with fluorinated vinyl ethers
Definitions
- This invention is in the field of melt-fabricable copolymers of tetrafluoroethylene.
- Carlson in U.S. Pat. No. 4,029,868 discloses certain copolymers of tetrafluoroethylene (TFE), hexafluoropropylene (HFP), and either perfluoro(propyl vinyl ether) (PPVE) or perfluoro(ethyl vinyl ether) (PEVE) having a flex life approaching or surpassing that of TFE/HFP copolymers.
- HFP concentration for Carlson's polymers was stated to be 4-12 wt % corresponding to HFP index (HFPI, the infrared measure of HFP content) of about 0.9-2.7.
- an insulating material be resistant to stress cracking in order that insulation made from the material have good integrity over time in service.
- High flex life is an indicator of good stress cracking resistance.
- Copolymers of tetrafluoroethylene, hexafluoropropylene, and perfluoro(methyl vinyl ether) having suitable combinations of hexafluoropropylene content and perfluoro(methyl vinyl ether) content have surprisingly good toughness as evidenced by flex life measurement.
- this invention provides a copolymer comprising tetrafluoroethylene, hexafluoropropylene in an amount corresponding to HFPI of from 1.9 to about 5.3, and an amount of perfluoro(methyl vinyl ether) effective to improve toughness, characterized by the copolymer exhibiting MIT Flex Life of at least 2000 cycles.
- the amount of perfluoro(methyl vinyl ether) is in the range 0.5-5% by weight.
- HFPI is determined by an infrared method outlined below.
- the copolymers contain an amount of PMVE that is effective to improve toughness over the corresponding TFE/HFP dipolymer.
- Toughness is characterized herein by flex life, and copolymers of this invention generally have MIT Flex Life of at least 2000 cycles, preferably at least 4000 cycles. These flex life values indicate that articles fabricated from the TFE/HFP/PMVE copolymer resin would have adequate resistance to stress cracking, depending on the use. As is well known in the art, stress cracking or brittleness is very much dependent on the thickness of an article in use. Copolymer having higher MIT Flex Life should be used for better toughness in thicker sections, whereas copolymer having lower MIT Flex Life can have equivalent toughness in thinner sections. Such thinner sections are encountered, for example, in films, in small-diameter wire insulations, and in cell walls of foam structures.
- PMVE content is in the range 0.5-5 wt %, preferably 0.5-3 wt %.
- PMVE content in the copolymer is determined by an infrared method, also outlined below.
- one or more additional copolymerizable monomers can be incorporated in the TFE/HFP/PMVE copolymers of this invention.
- the amount of such additional monomer will be such that the resultant copolymer remains partially crystalline, as indicated by detection of a melting endotherm by differential scanning calorimetry for resin as-polymerized, i.e., for resin that has not been previously melted.
- Copolymers of this invention generally have melt viscosity (MV) in the range 0.5-50 ⁇ 10 3 Pa.s. MV in the range 1-10 ⁇ 10 3 Pa.s is preferred.
- the TFE/HFP/PMVE copolymers of this invention can be made by any method of polymerization that yields generally homogeneous copolymer composition. Such methods include polymerization in aqueous media, polymerization in non-aqueous media, and polymerization in mixed media. Organic liquids used in the latter two polymerization systems commonly are halogenated compounds. In light of current environmental concerns about such compounds, aqueous dispersion polymerization is preferred. Such a process is disclosed, for example, for TFE/HFP/PPVE copolymer in SIR H130.
- aqueous polymerization For aqueous polymerization, a broad range of temperatures can be used. Because of the low reactivity of HFP relative to that of TFE, higher temperatures are advantageous, such as temperatures in the range of about 95°-115° C. Temperature in the range 98°-108° C. is preferred for making the copolymers of this invention by the aqueous semibatch process used in the examples below. Surfactants used in emulsion polymerization appear to be less effective at temperatures above 103°-108° C. and there is a tendency to lose dispersion stability.
- Surfactants suitable for use in dispersion polymerization of TFE/HFP copolymers can be used.
- Such surfactants include, for example, ammonium perfluorooctanoate (C-8), ammonium perfluorononanoate (C-9), and the perfluoroalkyl ethane sulfonic acids and salts thereof disclosed in U.S. Pat. No. 4,380,618.
- Initiators commonly employed in emulsion polymerization of TFE copolymers are water-soluble free-radical initiators such as ammonium persulfate (APS), potassium persulfate (KPS), or disuccinic acid peroxide. APS and/or KPS is preferred.
- an initiator solution which can be the same as or different from the first initiator solution, is usually added throughout the reaction.
- TFE/HFP copolymerization There are several alternatives for regulating the rate of TFE/HFP copolymerization, and these are applicable for polymerizing the TFE/HFP/PMVE copolymers of this invention. It is common with most alternatives first to precharge all HFP monomer and then to add TFE to the desired total pressure. Additional TFE is then added after initiator injection and reaction kickoff to maintain the chosen pressure. The TFE may be added at a constant rate, with agitator speed changed as necessary to increase or decrease actual polymerization rate and thus to maintain constant total pressure. Alternatively, the total pressure and the agitator speed may both be held constant, with TFE added as necessary to maintain the constant pressure. A third alternative is to carry out the polymerization in stages with variable agitator speed, but with steadily increasing TFE feed rates.
- the HFP monomer is much less reactive than the TFE monomer so that the HFP/TFE ratio must be kept high to assure a high incorporation of HFP.
- the PMVE can be incorporated into the copolymer by either pre-charge, pre-charge plus subsequent addition (pumping), or pumping of the PMVE into the reactor.
- the reactivity of PMVE relative to TFE is such that TFE/HFP/PMVE copolymer that is satisfactorily uniform with respect to PMVE incorporation can be obtained if PMVE is precharged to the reactor.
- Fluoropolymer compositions were determined on 0.095-0.105 mm thick films pressed at 300° C., using Fourier transform infrared spectroscopy.
- HFP determination the method described in U.S. Pat. No. 4,380,618 was used. In applying this method, the absorbances of bands found at about 10.18 ⁇ m and at about 4.25 ⁇ m were used. HFP content is expressed as an HFP index (HFPI), the ratio of the 10.18 ⁇ m absorbance to the 4.25 ⁇ m absorbance. HFP content in wt % was calculated as 3.2 ⁇ HFPI.
- PMVE was determined from an infrared band at 11.24 ⁇ m. PMVE content in wt % was calculated as 8 ⁇ the ratio of the 11.24 ⁇ m absorbance to 4.25 ⁇ m absorbance.
- Average size of polymer particles as polymerized i.e., raw dispersion particle size (RDPS) was measured by photon correlation spectroscopy.
- MIT Flex Life The standard MIT folding endurance tester described in ASTM D-2176 was used for determining flex life (MIT Flex Life). Measurements were made using compression-molded films that were quenched in cold water. Film thickness was 0.008 ⁇ 0.0005 inch (0.20 ⁇ 0.013 mm).
- solution concentrations are based on combined weight of solvent water and of solute(s).
- stated concentrations of polymer solids in dispersions are based on combined weights of solids and aqueous medium, and were determined gravimetrically, i.e., by weighing dispersion, drying, and weighing dried solids, or by an established correlation of dispersion specific gravity with the gravimetric method.
- a cylindrical, horizontal, water-jacketed, paddle-stirred, stainless steel reactor having a length to diameter ratio of about 1.5 and a water capacity of 80 parts by weight was charged with 50 parts of demineralized water and 0.36 part of a 20 wt % solution of ammonium perfluorooctanoate surfactant (C-8, Fluorad® FC-143, 3M) in water. With the reactor piddle agitated at 35 rpm, the reactor was heated to 65° C., evacuated, purged with TFE, and evacuated again. The reactor temperature then was increased to 103° C., and 0.4 part of liquid PMVE was injected into the reactor.
- C-8 ammonium perfluorooctanoate surfactant
- HFP was added slowly to the reactor until the pressure was 436 psig (3.1 MPa).
- TFE was added to the reactor to achieve a final pressure of 600 psig (4.2 MPa).
- 0.39 part of a freshly prepared aqueous initiator solution containing 0.80 wt % of ammonium persulfate (APS) and 0.80 wt % potassium persulfate (KPS) was charged into the reactor at 0.1 part/min. Then, this same initiator solution was pumped into the reactor at 0.015 part/min for the remainder of the polymerization.
- the dispersion Upon further cooling, the dispersion was discharged from the reactor at below 70° C. Solids content of the dispersion was 31.4 wt % and raw dispersion particle size (RDPS) was 0.167 ⁇ m.
- RDPS raw dispersion particle size
- the polymer was isolated by compressing excess water from the wet polymer and then drying this polymer in a 150° C. convection air oven.
- the TFE/HFP/PMVE terpolymer had an MV of 2.31 ⁇ 10 3 Pa.s, an HFPI of 4.03 (12.9 wt % HFP), a PMVE content of 1.30 wt %, and a melting point of 248° C. This polymer was stabilized by heating at 360° C.
- a film 0.005 inch thick would have approximately twice the flex life of a film 0.008 inch thick. This comparison indicates the toughening effect of PMVE in the copolymers of this invention.
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- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
Abstract
Description
TABLE 1 ______________________________________ Conditions and Results for Examples 2-4 Example: 2 3 4 ______________________________________ Run conditions: C-8 solution (part) nc 0.72 nc PMVE precharge (part) 0.17 0.33 0.20 HFP pressure (MPa) nc nc 2.5 Initiator pumping (part/min) 0.012 0.011 nc Dispersion properties: Solids (wt %) 27.7 31.7 25.4 RDPS (μm) 0.179 0.189 0.167 Resin properties: MV (10.sup.3 Pa · s) 6.40 6.73 8.44 HFPI 3.81 3.88 3.22 HFP content (wt %) 12.2 12.4 10.3 PMVE content (wt %) 0.58 1.06 0.89 Melting point (°C.) 243 247 251 MIT Flex Life (cycles) 14900 25000 9080 ______________________________________
Claims (4)
Priority Applications (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US08/678,919 US5688885A (en) | 1995-08-17 | 1996-07-12 | Tetrafluoroethylene terpolymer |
DE69610813T DE69610813T2 (en) | 1995-08-17 | 1996-08-12 | Tetrafluoroethylene terpolymer |
EP96112950A EP0789039B1 (en) | 1995-08-17 | 1996-08-12 | Tetrafluoroethylene terpolymer |
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US241095P | 1995-08-17 | 1995-08-17 | |
US08/678,919 US5688885A (en) | 1995-08-17 | 1996-07-12 | Tetrafluoroethylene terpolymer |
Publications (1)
Publication Number | Publication Date |
---|---|
US5688885A true US5688885A (en) | 1997-11-18 |
Family
ID=26670340
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
US08/678,919 Expired - Lifetime US5688885A (en) | 1995-08-17 | 1996-07-12 | Tetrafluoroethylene terpolymer |
Country Status (3)
Country | Link |
---|---|
US (1) | US5688885A (en) |
EP (1) | EP0789039B1 (en) |
DE (1) | DE69610813T2 (en) |
Cited By (21)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US6624269B2 (en) | 2000-06-23 | 2003-09-23 | Solvay Solexis S.P.A. | Tetrafluoroethylene thermoprocessable copolymer microspheres |
US6642307B1 (en) * | 1998-10-13 | 2003-11-04 | Daikin Industries, Ltd. | Process for producing fluoropolymer |
US6653379B2 (en) | 2001-07-12 | 2003-11-25 | 3M Innovative Properties Company | Fluoropolymers resistant to stress cracking |
US6703464B2 (en) | 2002-01-17 | 2004-03-09 | Daikin America, Inc. | Flourine-containing copolymer |
US6743508B2 (en) | 2002-01-17 | 2004-06-01 | Daikin America, Inc. | Fep pellet |
US20040204536A1 (en) * | 2001-06-18 | 2004-10-14 | Toshio Miyatani | Powder coating material |
US20090048359A1 (en) * | 2007-08-03 | 2009-02-19 | Glew Charles A | Compositions for compounding, extrusion and melt processing of foamable and cellular fluoropolymers |
US20100009075A1 (en) * | 2006-10-03 | 2010-01-14 | Chandler Blake E | Multi-layer articles and method for improving the release life of the same |
WO2012080098A1 (en) | 2010-12-16 | 2012-06-21 | Solvay Specialty Polymers Italy S.P.A. | Foamable fluoropolymer compositions |
WO2012084749A1 (en) | 2010-12-20 | 2012-06-28 | Solvay Specialty Polymers Italy S.P.A. | Thermoprocessable per(halo)fluoropolymer composition |
EP2631260A1 (en) | 2012-02-27 | 2013-08-28 | Solvay Sa | Process for Producing Graphene-Polymer Nanocomposites |
WO2015193321A1 (en) | 2014-06-19 | 2015-12-23 | Solvay Specialty Polymers Italy S.P.A. | Fluoropolymer composition |
WO2017102405A1 (en) | 2015-12-16 | 2017-06-22 | Solvay Specialty Polymers Italy S.P.A. | Multilayer assembly |
US10032542B2 (en) | 2014-11-07 | 2018-07-24 | Cable Components Group, Llc | Compositions for compounding, extrusion and melt processing of foamable and cellular halogen-free polymers |
US10031301B2 (en) | 2014-11-07 | 2018-07-24 | Cable Components Group, Llc | Compositions for compounding, extrusion, and melt processing of foamable and cellular polymers |
WO2018162401A1 (en) | 2017-03-10 | 2018-09-13 | Solvay Specialty Polymers Usa, Llc | Melt-processable composition |
WO2019096800A1 (en) | 2017-11-14 | 2019-05-23 | Solvay Specialty Polymers Italy S.P.A. | Multilayer assembly |
WO2019175197A1 (en) | 2018-03-15 | 2019-09-19 | Solvay Specialty Polymers Italy S.P.A. | Fluoropolymer composition for components of light emitting apparatus |
CN111171209A (en) * | 2018-11-12 | 2020-05-19 | 中昊晨光化工研究院有限公司 | Fluororesin and preparation method thereof |
WO2022148875A1 (en) | 2021-01-11 | 2022-07-14 | Solvay Specialty Polymers Italy S.P.A. | Fluoropolymer composition |
US11865758B2 (en) | 2017-06-26 | 2024-01-09 | Chemours-Mitsui Fluoroproducts Co. Ltd. | Fluororesin molded article |
Families Citing this family (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP4392706B2 (en) | 2000-02-02 | 2010-01-06 | 三井・デュポンフロロケミカル株式会社 | Heat-meltable fluororesin composition |
Citations (2)
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JPS5884874A (en) * | 1981-11-13 | 1983-05-21 | Du Pont Mitsui Fluorochem Co Ltd | Hot-melt adhesive for polytetrafluoroethylene molded product |
EP0117450A1 (en) * | 1983-02-01 | 1984-09-05 | Daikin Kogyo Co., Ltd. | Fluorine-containing copolymers |
Family Cites Families (3)
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BE560454A (en) | 1957-03-29 | |||
US4029868A (en) | 1976-03-10 | 1977-06-14 | E. I. Du Pont De Nemours And Company | Tetrafluoroethylene terpolymers |
US4380618A (en) | 1981-08-21 | 1983-04-19 | E. I. Du Pont De Nemours And Company | Batch polymerization process |
-
1996
- 1996-07-12 US US08/678,919 patent/US5688885A/en not_active Expired - Lifetime
- 1996-08-12 EP EP96112950A patent/EP0789039B1/en not_active Expired - Lifetime
- 1996-08-12 DE DE69610813T patent/DE69610813T2/en not_active Expired - Fee Related
Patent Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS5884874A (en) * | 1981-11-13 | 1983-05-21 | Du Pont Mitsui Fluorochem Co Ltd | Hot-melt adhesive for polytetrafluoroethylene molded product |
EP0117450A1 (en) * | 1983-02-01 | 1984-09-05 | Daikin Kogyo Co., Ltd. | Fluorine-containing copolymers |
Cited By (47)
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US6642307B1 (en) * | 1998-10-13 | 2003-11-04 | Daikin Industries, Ltd. | Process for producing fluoropolymer |
US20040082746A1 (en) * | 2000-06-23 | 2004-04-29 | Ausimont S.P.A. | Tetrafluoroethylene thermoprocessable copolymer microspheres |
US6624269B2 (en) | 2000-06-23 | 2003-09-23 | Solvay Solexis S.P.A. | Tetrafluoroethylene thermoprocessable copolymer microspheres |
US6809167B2 (en) | 2000-06-23 | 2004-10-26 | Ausimont S.P.A. | Tetrafluoroethylene thermoprocessable copolymer microspheres |
US20040204536A1 (en) * | 2001-06-18 | 2004-10-14 | Toshio Miyatani | Powder coating material |
US20040072935A1 (en) * | 2001-07-12 | 2004-04-15 | 3M Innovative Properties Company | Fluoropolymers resistant to stress cracking |
US6984697B2 (en) | 2001-07-12 | 2006-01-10 | 3M Innovative Properties Company | Fluoropolymers resistant to stress cracking |
US6653379B2 (en) | 2001-07-12 | 2003-11-25 | 3M Innovative Properties Company | Fluoropolymers resistant to stress cracking |
US7105619B2 (en) | 2002-01-17 | 2006-09-12 | Daikin Industries, Ltd. | Fluorine-containing copolymer |
US20050049375A1 (en) * | 2002-01-17 | 2005-03-03 | Hideki Kono | Fluorine-containing copolymer |
US20050118431A1 (en) * | 2002-01-17 | 2005-06-02 | Daikin Industries, Ltd. Umeda Center Building | Fep pellet |
US6703464B2 (en) | 2002-01-17 | 2004-03-09 | Daikin America, Inc. | Flourine-containing copolymer |
US6743508B2 (en) | 2002-01-17 | 2004-06-01 | Daikin America, Inc. | Fep pellet |
US20070243388A1 (en) * | 2002-01-17 | 2007-10-18 | Daikin Industries, Ltd. | FEP pellet |
US8334351B2 (en) | 2002-01-17 | 2012-12-18 | Daikin Industries, Ltd. | FEP pellet |
US7923519B2 (en) | 2002-01-17 | 2011-04-12 | Daikin Industries, Ltd. | FEP pellet |
US20110209896A1 (en) * | 2002-01-17 | 2011-09-01 | Daikin Industries, Ltd. | Fep pellet |
US20100009075A1 (en) * | 2006-10-03 | 2010-01-14 | Chandler Blake E | Multi-layer articles and method for improving the release life of the same |
US8007863B2 (en) * | 2006-10-03 | 2011-08-30 | 3M Innovative Properties Company | Multi-layer articles and method for improving the release life of the same |
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US20110224318A1 (en) * | 2007-08-03 | 2011-09-15 | Cable Components Group Llc | Compositions for Compounding, Extrusion and Melt Processing of Foamable and Cellular Fluoropolymers |
US20100072644A1 (en) * | 2007-08-03 | 2010-03-25 | Cable Components Group | Compositions, additives, and compounds for melt processable, foamable, and cellular fluoroploymers |
US7968613B2 (en) | 2007-08-03 | 2011-06-28 | Cable Components Group Llc | Compositions for compounding, extrusion and melt processing of foamable and cellular fluoropolymers |
US8912243B2 (en) | 2007-08-03 | 2014-12-16 | Cable Components Group, Llc | Compositions, additives, and compounds for melt processable, foamable, and cellular fluoroploymers |
US8278366B2 (en) | 2007-08-03 | 2012-10-02 | Cable Components Group Llc | Compositions for compounding, extrusion and melt processing of foamable and cellular fluoropolymers |
US8318819B2 (en) | 2007-08-03 | 2012-11-27 | Cable Components Group, Llc | Compositions for compounding foamable, fluropolymer pellets for use in melt processing cellular or foamed fluoropolymer applications |
US20090048359A1 (en) * | 2007-08-03 | 2009-02-19 | Glew Charles A | Compositions for compounding, extrusion and melt processing of foamable and cellular fluoropolymers |
WO2012080098A1 (en) | 2010-12-16 | 2012-06-21 | Solvay Specialty Polymers Italy S.P.A. | Foamable fluoropolymer compositions |
US10246572B2 (en) | 2010-12-16 | 2019-04-02 | Solvay Specialty Polymers Italy S.P.A. | Foamable fluoropolymer compositions |
WO2012084749A1 (en) | 2010-12-20 | 2012-06-28 | Solvay Specialty Polymers Italy S.P.A. | Thermoprocessable per(halo)fluoropolymer composition |
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WO2015193321A1 (en) | 2014-06-19 | 2015-12-23 | Solvay Specialty Polymers Italy S.P.A. | Fluoropolymer composition |
US10308830B2 (en) | 2014-06-19 | 2019-06-04 | Solvay Specialty Polymers Italy S.P.A. | Fluoropolymer composition |
US10825580B2 (en) | 2014-11-07 | 2020-11-03 | Cable Components Group, Llc | Compositions for compounding, extrusion and melt processing of foamable and cellular halogen-free polymers |
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US10032542B2 (en) | 2014-11-07 | 2018-07-24 | Cable Components Group, Llc | Compositions for compounding, extrusion and melt processing of foamable and cellular halogen-free polymers |
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US11865758B2 (en) | 2017-06-26 | 2024-01-09 | Chemours-Mitsui Fluoroproducts Co. Ltd. | Fluororesin molded article |
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WO2019175197A1 (en) | 2018-03-15 | 2019-09-19 | Solvay Specialty Polymers Italy S.P.A. | Fluoropolymer composition for components of light emitting apparatus |
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Also Published As
Publication number | Publication date |
---|---|
EP0789039A1 (en) | 1997-08-13 |
DE69610813D1 (en) | 2000-12-07 |
EP0789039B1 (en) | 2000-11-02 |
DE69610813T2 (en) | 2001-06-21 |
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Owner name: JPMORGAN CHASE BANK, N.A., NEW YORK Free format text: SECURITY AGREEMENT;ASSIGNORS:THE CHEMOURS COMPANY FC LLC;THE CHEMOURS COMPANY TT, LLC;REEL/FRAME:035839/0675 Effective date: 20150512 |
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AS | Assignment |
Owner name: THE CHEMOURS COMPANY FC, LLC, DELAWARE Free format text: RELEASE BY SECURED PARTY;ASSIGNOR:JPMORGAN CHASE BANK, N.A., AS ADMINISTRATIVE AGENT;REEL/FRAME:045845/0913 Effective date: 20180403 |